SLC16A3 — 108 ClinVar variants

All ClinVar germline SLC16A3 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 86 flagged for review →

2 Benign · 15 Likely benign · 91 Uncertain significance

Full SLC16A3 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions

⚑ Evidence disagreements 86

Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.

Predictors lean, ClinVar uncertain 66

ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.

All SLC16A3 variants

Benign 2

Likely benign 15

Uncertain significance 91